ClinVar Miner

Submissions for variant NM_003803.4(MYOM1):c.2506+15C>G

dbSNP: rs1272570164
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000605563 SCV000712308 likely benign not specified 2016-08-04 criteria provided, single submitter clinical testing c.2506+15C>G in intron 17 of MYOM1: This variant is not expected to have clinica l significance because it is not located within the splice consensus sequence.

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